Heiko Schoof

dblp:71/5274 · DBLP profile ↗
← Back
3ranked-venue papers
0as first author
1since 2021 · last 2022
0000-0002-1527-3752ORCID · corroborated

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 3 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
3 papers
Bioinformatics and computational biology · 100%

Topics — the 6 heaviest of 6, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
functional genomics
0.612022
MuWU: Mutant-seq library analysis and annotation · Bioinform. 2022
Bioinformatics and computational biology › genomics › computational genomics
gene prioritization
0.112012
Marker2sequence, mine your QTL regions for candidate genes · Bioinform. 2012
Bioinformatics and computational biology › multi-omics data integration
genomic data integration
0.112012
Marker2sequence, mine your QTL regions for candidate genes · Bioinform. 2012
Bioinformatics and computational biology › genome annotation
automatic annotation
0.112008
Protein function prediction and annotation in an integrated environment powered by web services (AFAWE) · Bioinform. 2008
Bioinformatics and computational biology
protein function prediction
0.112008
Protein function prediction and annotation in an integrated environment powered by web services (AFAWE) · Bioinform. 2008
Bioinformatics and computational biology › statistical genetics
quantitative trait locus analysis
0.012012
Marker2sequence, mine your QTL regions for candidate genes · Bioinform. 2012

Methods — techniques the papers use, named apart from their topics

workflow pipeline · 0.6keyword-based filtering · 0.1data integration · 0.1workflow integration · 0.1web services · 0.1
YearPublicationVenuePosition
2022 MuWU: Mutant-seq library analysis and annotation
abstract
MOTIVATION: Insertional mutagenesis allows for the creation of loss-of-function mutations on a genome-wide scale. In theory, every gene can be 'knocked out' via the insertion of an additional DNA sequence. Resources of sequence-indexed mutants of plant and animal model organisms are instrumental for functional genomics studies. Such repositories significantly speed up the acquisition of interesting genotypes and allow for the validation of hypotheses regarding phenotypic consequences in reverse genetics. To create such resources, comprehensive sequencing of flanking sequence tags using protocols such as Mutant-seq requires various downstream computational tasks, and these need to be performed in an efficient and reproducible manner. RESULTS: Here, we present MuWU, an automated Mutant-seq workflow utility initially created for the identification of Mutator insertion sites of the BonnMu resource, representing a reverse genetics mutant collection for functional genetics in maize (Zea mays). MuWU functions as a fast, one-stop downstream processing pipeline of Mutant-seq reads. It takes care of all complex bioinformatic tasks, such as identifying tagged genes and differentiating between germinal and somatic mutations/insertions. Furthermore, MuWU automatically assigns insertions to the corresponding mutated seed stocks. We discuss the implementation and how parameters can easily be adapted to use MuWU for other species/transposable elements. AVAILABILITY AND IMPLEMENTATION: MuWU is a Snakemake-based workflow and freely available at https://github.com/tgstoecker/MuWU. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Tyll Stöcker, Lena Altrogge, Caroline Marcon, Yan Naing Win, Frank Hochholdinger, Heiko Schoof
Bioinform.6
2012 Marker2sequence, mine your QTL regions for candidate genes
abstract
UNLABELLED: Marker2sequence (M2S) aims at mining quantitative trait loci (QTLs) for candidate genes. For each gene, within the QTL region, M2S uses data integration technology to integrate putative gene function with associated gene ontology terms, proteins, pathways and literature. As a typical QTL region easily contains several hundreds of genes, this gene list can then be further filtered using a keyword-based query on the aggregated annotations. M2S will help breeders to identify potential candidate genes for their traits of interest. AVAILABILITY: Marker2sequence is freely accessible at http://www.plantbreeding.wur.nl/BreeDB/marker2seq/. The source code can be obtained at https://github.com/PBR/Marker2Sequence. CONTACT: [email protected]
Pierre-Yves Chibon, Heiko Schoof, Richard G. F. Visser, Richard Finkers
Bioinform.2
2008 Protein function prediction and annotation in an integrated environment powered by web services (AFAWE)
abstract
Abstract Summary: Many sequenced genes are mainly annotated through automatic transfer of annotation from similar sequences. Manual comparison of results or intermediate results from different tools can help avoid wrong annotations and give hints to the function of a gene even if none of the automated tools could return any result. AFAWE simplifies the task of manual functional annotation by running different tools and workflows for automatic function prediction and displaying the results in a way that facilitates comparison. Because all programs are executed as web services, AFAWE is easily extensible and can directly query primary databases, thereby always using the most up-to-date data sources. Visual filters help to distinguish trustworthy results from non-significant results. Furthermore, an interface to add detailed manual annotation to each gene is provided, which can be displayed to other users. Availability: AFAWE is available at http://bioinfo.mpiz-koeln.mpg.de/afawe/ Contact: [email protected] Supplementary information: SIFTER pipeline (S1), AFAWE tutorial (S2).
Anika Jöcker, Fabian Hoffmann, Andreas Groscurth, Heiko Schoof
Bioinform.4